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Symbol
Name
ID
Arl13b
ADP-ribosylation factor-like 13B
MGI:1915396
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Occipital encephalocele
Oculomotor apraxia
Molar tooth sign on MRI
Ataxia
Intellectual disability
Global developmental delay
Disease(s) Associated with ARL13B
Joubert syndrome 8

Mouse Phenotypes
absent floor plate
spina bifida
Availability Mouse Genotype
Arl13bhnn/Arl13bhnn

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
09/17/2019
MGI 6.14
The Jackson Laboratory